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Unique clinical and serological features of bullous pemphigoid associated with dipeptidyl peptidase‐4 inhibitors

British journal of dermatology (1951), 2018-06, Vol.178 (6), p.1462-1463

2018

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A nonepidermolytic keratinocytic epidermal naevus associated with a postzygotic mutation in the gene encoding epidermal growth factor receptor

British journal of dermatology (1951), 2020-05, Vol.182 (5), p.1303-1305

2020

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Identification of factors contributing to phenotypic divergence via quantitative image analyses of autosomal recessive woolly hair/hypotrichosis with homozygous c.736T>A LIPH mutation

British journal of dermatology (1951), 2017-01, Vol.176 (1), p.138-144

2017

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Alopecia areata multiplex following autologous dermal micrograft injection for treatment of androgenetic alopecia

Journal of the European Academy of Dermatology and Venereology, 2019-11, Vol.33 (11), p.e397-e399

2019

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Authors’ reply to: Comment on the article by Dr. Toshima about alopecia areata multiplex following autologous dermal micrograft injection

Journal of the European Academy of Dermatology and Venereology, 2020-05, Vol.34 (5), p.e222-e223

2020

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Azathioprine‐induced alopecia and leukopenia associated with NUDT15 polymorphisms

Journal of the European Academy of Dermatology and Venereology, 2018-10, Vol.32 (10), p.e386-e389

2018

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Distinct phenotype of epidermolysis bullosa simplex with infantile migratory circinate erythema due to frameshift mutations in the V2 domain of KRT5

Journal of the European Academy of Dermatology and Venereology, 2017-05, Vol.31 (5), p.e241-e243

2017

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Diminished regulatory T cells in cutaneous lesions of thymoma‐associated multi‐organ autoimmunity: a newly described paraneoplastic autoimmune disorder with fatal clinical course

Clinical and experimental immunology, 2011-11, Vol.166 (2), p.164-170

2011

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Vörner type palmoplantar keratoderma: novel KRT9 mutation associated with knuckle pad-like lesions and recurrent mutation causing digital mutilation

British journal of dermatology (1951), 2011-07, Vol.165 (1), p.199-201

2011

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A Case of Generalized Acanthosis Nigricans with Positive Lupus Erythematosus-Related Autoantibodies and Antimicrosomal Antibody: Autoimmune Acanthosis Nigricans

Case reports in dermatology, 2012-03, Vol.4 (1), p.85-91

2012

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Oral steroid improves bullous pemphigoid‐like clinical manifestations in non‐Herlitz junctional epidermolysis bullosa with COL17A1 mutation

British journal of dermatology (1951), 2007-09, Vol.157 (3), p.596-598

2007

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The course of pregnancy and childbirth in three mothers with recessive dystrophic epidermolysis bullosa

Clinical and experimental dermatology, 2012-01, Vol.37 (1), p.10-14

2012

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Novel and recurrent nonsense mutation of the SLC39A4 gene in Japanese patients with acrodermatitis enteropathica

British journal of dermatology (1951), 2009-07, Vol.161 (1), p.184-186

2009

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A marked decrease in bispectral index with elevation of suppression ratio by cervical haematoma reducing cerebral perfusion pressure

Journal of clinical neuroscience, 2003-11, Vol.10 (6), p.694-696

2003

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821 A non-epidermolytic epidermal nevus associated with a postzygotic EGFR mutation

Journal of investigative dermatology, 2023-05, Vol.143 (5), p.S141-S141

2023

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Photodynamic therapy may be useful in debulking cutaneous lymphoma prior to radiotherapy

Clinical and experimental dermatology, 2004-01, Vol.29 (1), p.42-45

2004

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A case of bullous pemphigoid exacerbated by irradiation after breast conservative radiotherapy

Japanese journal of clinical oncology, 2011-06, Vol.41 (6), p.811-813

2011

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195 The identification of a postzygotic GJA1 mutation in a patient with an inflammatory linear verrucous epidermal nevus suggests that the disease is a mosaic of erythrokeratodermia variabilis et progressiva

Journal of investigative dermatology, 2017-10, Vol.137 (10), p.S226-S226

2017

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Effect of Helicobacter pylori eradication in the treatment of Japanese patients with chronic idiopathic urticaria

Journal of gastroenterology, 2004-09, Vol.39 (9), p.827-830

2004

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Vörner type palmoplantar keratoderma: novel KRT9 mutation associated with knuckle pad-like lesions and recurrent mutation causing digital mutilation: Correspondence

British journal of dermatology (1951), 2011-07, Vol.165 (1), p.199-201

2011

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Vöner type palmoplantar keratoderma: novel KRT9 mutation associated with knuckle padlike lesions and recurrent mutation causing digital mutilation

British journal of dermatology (1951), 2011, Vol.165 (1), p.199-201

2011

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Hereditary Angjoedema in Japan: Genetic Analysis of 13 Unrelated Cases

The American journal of the medical sciences, 2012-03, Vol.343 (3), p.210-214

2012

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Azathioprine‐induced alopecia and leukopenia associated with NUDT 15 polymorphisms

Journal of the European Academy of Dermatology and Venereology, 2018-10, Vol.32 (10)

2018

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The course of pregnancy and childbirth in three mothers with recessive dystrophic epidermolysis bullosa: Pregnancy and childbirth in RDEB

Clinical and experimental dermatology, 2012-01, Vol.37 (1), p.10-14

2012

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Distinct phenotype of epidermolysis bullosa simplex with infantile migratory circinate erythema due to frameshift mutations in the V2 domain of KRT 5

Journal of the European Academy of Dermatology and Venereology, 2017-05, Vol.31 (5)

2017

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Unique clinical and serological features of bullous pemphigoid associated with dipeptidyl peptidase‐4 inhibitors

A nonepidermolytic keratinocytic epidermal naevus associated with a postzygotic mutation in the gene encoding epidermal growth factor receptor

Identification of factors contributing to phenotypic divergence via quantitative image analyses of autosomal recessive woolly hair/hypotrichosis with homozygous c.736T>A LIPH mutation

Alopecia areata multiplex following autologous dermal micrograft injection for treatment of androgenetic alopecia

Authors’ reply to: Comment on the article by Dr. Toshima about alopecia areata multiplex following autologous dermal micrograft injection

Azathioprine‐induced alopecia and leukopenia associated with NUDT15 polymorphisms

Distinct phenotype of epidermolysis bullosa simplex with infantile migratory circinate erythema due to frameshift mutations in the V2 domain of KRT5

Diminished regulatory T cells in cutaneous lesions of thymoma‐associated multi‐organ autoimmunity: a newly described paraneoplastic autoimmune disorder with fatal clinical course

Vörner type palmoplantar keratoderma: novel KRT9 mutation associated with knuckle pad-like lesions and recurrent mutation causing digital mutilation

A Case of Generalized Acanthosis Nigricans with Positive Lupus Erythematosus-Related Autoantibodies and Antimicrosomal Antibody: Autoimmune Acanthosis Nigricans

Oral steroid improves bullous pemphigoid‐like clinical manifestations in non‐Herlitz junctional epidermolysis bullosa with COL17A1 mutation

The course of pregnancy and childbirth in three mothers with recessive dystrophic epidermolysis bullosa

Novel and recurrent nonsense mutation of the SLC39A4 gene in Japanese patients with acrodermatitis enteropathica

A marked decrease in bispectral index with elevation of suppression ratio by cervical haematoma reducing cerebral perfusion pressure

821 A non-epidermolytic epidermal nevus associated with a postzygotic EGFR mutation

Photodynamic therapy may be useful in debulking cutaneous lymphoma prior to radiotherapy

A case of bullous pemphigoid exacerbated by irradiation after breast conservative radiotherapy

195 The identification of a postzygotic GJA1 mutation in a patient with an inflammatory linear verrucous epidermal nevus suggests that the disease is a mosaic of erythrokeratodermia variabilis et progressiva

Effect of Helicobacter pylori eradication in the treatment of Japanese patients with chronic idiopathic urticaria

Vörner type palmoplantar keratoderma: novel KRT9 mutation associated with knuckle pad-like lesions and recurrent mutation causing digital mutilation: Correspondence

Vöner type palmoplantar keratoderma: novel KRT9 mutation associated with knuckle padlike lesions and recurrent mutation causing digital mutilation

Hereditary Angjoedema in Japan: Genetic Analysis of 13 Unrelated Cases

Azathioprine‐induced alopecia and leukopenia associated with NUDT 15 polymorphisms

The course of pregnancy and childbirth in three mothers with recessive dystrophic epidermolysis bullosa: Pregnancy and childbirth in RDEB

Distinct phenotype of epidermolysis bullosa simplex with infantile migratory circinate erythema due to frameshift mutations in the V2 domain of KRT 5

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